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Catalog Number:
40324
CAS Number:
100379-00-8
2,6-Dimethylphenylboronic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
2,6-Dimethylbenzeneboronic acid, m-Xylene-2-boronic acid
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Product Information

2,6-Dimethylphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valued for its ability to form stable complexes with diols, making it an essential reagent in the development of various pharmaceuticals and agrochemicals. Its unique structure allows for selective reactions, which are crucial in the synthesis of complex organic molecules. Researchers often employ 2,6-Dimethylphenylboronic acid in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds that are fundamental in the creation of diverse chemical entities.

In addition to its applications in synthetic chemistry, 2,6-Dimethylphenylboronic acid has shown promise in the field of sensor technology, particularly in the detection of glucose and other biomolecules. Its ability to interact with sugars makes it a valuable component in the development of biosensors, which are increasingly important in medical diagnostics and environmental monitoring. With its broad range of applications and the potential for innovation in various fields, 2,6-Dimethylphenylboronic acid stands out as a key compound for researchers and industry professionals alike.

Synonyms
2,6-Dimethylbenzeneboronic acid, m-Xylene-2-boronic acid
CAS Number
100379-00-8
Purity
≥ 98% (HPLC)
Molecular Formula
C8H11BO2
Molecular Weight
149.98
MDL Number
MFCD01009693
PubChem ID
583322
Melting Point
105 °C (dec.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
2,6-Dimethylbenzeneboronic acid, m-Xylene-2-boronic acid
CAS Number
100379-00-8
Purity
≥ 98% (HPLC)
Molecular Formula
C8H11BO2
Molecular Weight
149.98
MDL Number
MFCD01009693
PubChem ID
583322
Melting Point
105 °C (dec.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2,6-Dimethylphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key reagent in Suzuki coupling reactions, enabling the formation of carbon-carbon bonds essential for creating complex organic molecules.
  • Pharmaceutical Development: It plays a critical role in the synthesis of various pharmaceutical intermediates, particularly in the development of anti-cancer and anti-inflammatory drugs.
  • Material Science: Used in the production of boron-containing polymers, it enhances material properties, making them suitable for applications in electronics and coatings.
  • Bioconjugation: Its ability to form stable complexes with sugars makes it valuable in bioconjugation processes, facilitating the development of targeted drug delivery systems.
  • Sensor Technology: This compound is utilized in the design of sensors for detecting biomolecules, offering high sensitivity and selectivity in various analytical applications.

Citations